Gene >> PTGS1
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000362012 |
| Start |
122386662:122386662(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1226A>T |
| AA Mutation |
p.Asn409Ile(p.N409I) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant;splice_region_variant |
| Transcription ID |
ENST00000362012 |
| Start |
122378775:122378775(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.353T>G |
| AA Mutation |
p.Val118Gly(p.V118G) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |